Blancard Corinne, Decoeur Fanny, Duvezin-Caubet Stéphane, Giraud Marie-France, Salin Bénédicte
University of Bordeaux, CNRS, IBGC, Bordeaux, France.
University of Bordeaux, CNRS, INSERM, BIC, Bordeaux, France.
Biol Cell. 2025 Jan;117(1):e2400038. doi: 10.1111/boc.202400038. Epub 2024 Dec 8.
Conventional Transmission Electron Microscopy analysis of biological samples often provides limited insights due to its inherent two-dimensional (2D) nature. This limitation hampers a comprehensive understanding of the three-dimensional (3D) complexity of cellular structures, occasionally leading to misinterpretations. Serial block-face scanning electron microscopy emerges as a powerful method for acquiring high-resolution 3D images of cellular volumes. By iteratively removing ultrathin sample sections and capturing images of each newly exposed surface, Serial block-face scanning electron microscopy allows for the meticulous reconstruction of a comprehensive 3D volume.
In this study, we investigate the 3D architecture of altered mitochondrial morphologies in Saccharomyces cerevisiae using Serial block-face scanning electron microscopy imaging. We have developed a novel cryomethod based on plunge freezing and a dedicated freeze-substitution protocol.
This protocol enhances ultrastructural preservation enabling a more accurate understanding of mitochondrial defects observed in 2D electron microscopy.
Our findings underscore the utility of Serial block-face scanning electron microscopy coupled with optimized sample preparation techniques in elucidating complex cellular structures in 3D.
由于传统的生物样本透射电子显微镜分析具有固有的二维(2D)特性,其提供的见解往往有限。这一局限性阻碍了对细胞结构三维(3D)复杂性的全面理解,偶尔会导致误解。连续块面扫描电子显微镜成为获取细胞体积高分辨率3D图像的有力方法。通过迭代去除超薄样本切片并捕获每个新暴露表面的图像,连续块面扫描电子显微镜能够精细重建完整的3D体积。
在本研究中,我们使用连续块面扫描电子显微镜成像研究酿酒酵母中线粒体形态改变的3D结构。我们开发了一种基于骤冷冷冻的新型冷冻方法和专门的冷冻替代方案。
该方案增强了超微结构的保存,能够更准确地理解在二维电子显微镜中观察到的线粒体缺陷。
我们的研究结果强调了连续块面扫描电子显微镜与优化的样本制备技术相结合在阐明3D复杂细胞结构方面的实用性。